Literature DB >> 14736542

Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo.

Xiao-Li Tian1, Sandro L Yong, Xiaoping Wan, Ling Wu, Mina K Chung, Patrick J Tchou, David S Rosenbaum, David R Van Wagoner, Glenn E Kirsch, Qing Wang.   

Abstract

OBJECTIVE: Mutations in the cardiac sodium channel gene SCN5A are responsible for type-3 long QT disease (LQT3). The genesis of cardiac arrhythmias in LQT3 is multifaceted, and the aim of this study was to further explore mechanisms by which SCN5A mutations lead to arrhythmogenesis in vivo.
METHODS: We engineered selective cardiac expression of a long QT syndrome (LQTS) mutation (N1325S) in human SCN5A and generated a transgenic mouse model, TGM(NS31).
RESULTS: Conscious and unrestrained TGM(NS31)L12 mice demonstrated a significant prolongation of the QT-interval and a high incidence of spontaneous polymorphic ventricular tachycardia (VT) and fibrillation (VF), often resulting in sudden cardiac death (n=52:156). Arrhythmias were suppressed by mexiletine, a sodium channel blocker for the late persistent sodium current. Action potentials (APs) from TGM(NS31)L12 ventricular myocytes exhibited early afterdepolarizations and longer 90% AP durations (APD90=69 +/- 5.9 ms) than control (APD90=46.7 +/- 4.8 ms). Voltage-clamp experiments in transgenic myocytes revealed a peak inward sodium current (INa) followed by a slow recovery from inactivation. After mexiletine application, transgenic ventricular APDs were shortened, and recovery from inactivation of INa was enhanced. These suggest that the N1325S transgene is responsible for the abnormal signals present in transgenic cells as well as the genesis of lethal arrhythmias in mice. Interestingly, transgenic but not wild-type myocytes displayed longer APDs with a shortening of CLs.
CONCLUSIONS: Our findings show that a new model for LQTS has been established, and we report on an arrhythmogenic mechanism that, unlike other SCN5A mutations, results in poor restitution of APD with increasing rate as a possible substrate for arrhythmogenesis.

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Year:  2004        PMID: 14736542      PMCID: PMC1579709          DOI: 10.1016/j.cardiores.2003.11.007

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  23 in total

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  37 in total

1.  Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes.

Authors:  Sandro L Yong; Ying Ni; Teng Zhang; David J Tester; Michael J Ackerman; Qing K Wang
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7.  Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3.

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9.  Induction of high STAT1 expression in transgenic mice with LQTS and heart failure.

Authors:  Ling Wu; Stephen R Archacki; Teng Zhang; Qing K Wang
Journal:  Biochem Biophys Res Commun       Date:  2007-04-26       Impact factor: 3.575

10.  LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in mice.

Authors:  Teng Zhang; Sandro L Yong; Jeanne K Drinko; Zoran B Popović; John C Shryock; Luiz Belardinelli; Qing Kenneth Wang
Journal:  Int J Cardiol       Date:  2009-09-17       Impact factor: 4.164

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